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  Vol. 101 No. 8, August 1983 TABLE OF CONTENTS
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Butterfly-Shaped Macular Dystrophy in Four Generations

Jay G. Prensky, MD; George H. Bresnick, MD

Arch Ophthalmol. 1983;101(8):1198-1203.


Abstract

• Four generations in a family were affected by butterfly-shaped macular dystrophy. Affected members ranged in age from 8 to 77 years. In addition to the primary features of autosomal dominant inheritance, bilateral symmetrical pigmented macular lesion, and a low electrooculographic light peak-dark trough ratio, we discovered additional progressive changes: peripapillary and parafoveal chorioretinal atrophy, enlarged blind spots, and paracentral scotomas with diminished visual acuity late. Because of the progressive change in the ophthalmologic appearance of the fundus, the diagnosis could easily be overlooked in advanced cases.



Author Affiliations

From the Department of Ophthalmology, University of Wisconsin Medical School, Madison.


Footnotes

Accepted for publication June 29, 1982.

Read in part at the Retina Society Annual Meeting, San Francisco, Sept 19, 1981.

Reprint requests to Department of Ophthalmology, Box F4/3, University of Wisconsin Center for Health Sciences, 600 Highland Ave, Madison, WI 53792 (Dr Bresnick).



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Mutations in the peripherin/RDS gene are an important cause of multifocal pattern dystrophy simulating STGD1/fundus flavimaculatus
Boon et al.
Br J Ophthalmol 2007;91:1504-1511.
ABSTRACT | FULL TEXT  

Butterfly-Shaped Pattern Dystrophy: A Genetic, Clinical, and Histopathological Report
Zhang et al.
Arch Ophthalmol 2002;120:485-490.
ABSTRACT | FULL TEXT  

Deletion in the Peripherin/RDS Gene in Two Unrelated Sardinian Families With Autosomal Dominant Butterfly-Shaped Macular Dystrophy
Fossarello et al.
Arch Ophthalmol 1996;114:448-456.
ABSTRACT  





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